US2008032232A1PendingUtilityA1
Novel resins and photoresist compositions comprising same
Est. expiryMay 30, 2022(expired)· nominal 20-yr term from priority
Y10S430/106G03F 7/0382G03F 7/0397G03F 7/004
36
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Claims
Abstract
Provided are new resins that comprise carbocyclic aryl units with hetero substitution units and photoresists that contain such resins. Particularly preferred photoresists of the invention comprise a deblocking resin that contains hydroxy naphthyl units and can be effectively imaged with sub-200 nm radiation such as 193 nm radiation.
Claims
exact text as granted — not AI-modified1 - 68 . (canceled)
69 . A method for providing a photoresist relief image, comprising:
a) applying a coating layer of a positive-acting photoresist composition on a substrate, the photoresist composition comprising a photoactive component and a tetrapolymer or pentapolymer that comprises hetero-substituted multi-ring carbocyclic aryl groups; and b) exposing the photoresist composition layer to activating radiation having a wavelength of less than 200 nm and developing the exposed photoresist composition coating layer.
70 . The method of claim 69 wherein the photoresist layer is exposed to radiation having a wavelength of about 193 nm.
71 . The method of claim 69 wherein the tetrapolymer or pentapolymer has a weight average molecular weight of from greater than 2,000 to about 100,000.
72 . The method of claim 69 wherein the tetrapolymer or pentapolymer comprises hetero-substituted naphthyl groups.
73 . The method of claim 69 wherein the tetrapolymer or pentapolymer comprises units containing hydroxy naphthyl groups.
74 . The method of claim 69 wherein the photoresist composition comprises a tetrapolymer that comprises hetero-substituted multi-ring carbocyclic aryl groups.
75 . The method of claim 69 wherein the photoresist composition comprises a pentapolymer that comprises hetero-substituted multi-ring carbocyclic aryl groups.
76 . The method of claim 69 wherein the tetrapolymer or pentapolymer comprises photoacid-labile groups.
77 . The method of claim 69 wherein the tetrapolymer or pentapolymer comprises polymerized acrylate units.
78 . The method of claim 69 wherein the tetrapolymer or pentapolymer comprises lactone groups.
79 . A photoresist composition comprising a photoactive component and a tetrapolymer or pentapolymer that comprises hetero-substituted multi-ring carbocyclic aryl groups.
80 . The photoresist composition of claim 79 wherein the tetrapolymer or pentapolymer has a weight average molecular weight of from greater than 2,000 to about 100,000.
81 . The photoresist composition of claim 79 wherein the tetrapolymer or pentapolymer comprises hetero-substituted naphthyl groups.
82 . The photoresist composition of claim 79 wherein the tetrapolymer or pentapolymer comprises units containing hydroxy naphthyl groups.
83 . The photoresist composition method of claim 79 wherein the photoresist composition comprises a tetrapolymer that comprises hetero-substituted multi-ring carbocyclic aryl groups.
84 . The photoresist composition of claim 79 wherein the photoresist composition comprises a pentapolymer that comprises hetero-substituted multi-ring carbocyclic aryl groups.
85 . The photoresist composition method of claim 75 wherein the tetrapolymer or pentapolymer comprises photoacid-labile groups.
86 . The photoresist composition of claim 79 wherein the tetrapolymer or pentapolymer comprises polymerized acrylate units.
87 . The photoresist composition of claim 79 wherein the tetrapolymer or pentapolymer comprises lactone groups.
88 . The photoresist composition of claim 79 wherein the tetrapolymer or pentapolymer is substantially free of aromatic groups other than the hetero-substituted carbocyclic aryl groups.Cited by (0)
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